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Medical Writer III, Oncology

usd87k - usd140.3k per year

Johnson & Johnson

Medical Writer III focused on oncology regulatory documentation within Johnson & Johnson's Innovative Medicine division. The role involves writing and coordinating clinical and regulatory documents, leading cross-functional teams, and mentoring junior staff across a hybrid work model in multiple global locations.

Responsibilities

  • Write and coordinate clinical and regulatory documents including CSRs, IBs, protocols, and regulatory responses
  • Lead cross-functional document planning and review meetings with clinical and regulatory teams
  • Function as primary lead writer on most compounds under supervision
  • Coach and mentor junior medical writing staff on processes, content, and best practices
  • Participate in or lead process working groups and establish document timelines

Requirements

  • University degree in scientific discipline; advanced degree preferred
  • Minimum 6 years pharmaceutical/scientific industry experience with 4+ years regulatory medical writing
  • Oncology therapeutic area experience preferred
  • Ability to interpret and present statistical and medical information in complex documents
  • Compound lead and/or submission lead experience preferred
  • Proficiency in written and spoken English with global collaboration capability
  • Strong leadership, project management, and problem-solving skills
Vacancy posted 1 day ago
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